Title of article :
mTOR pathway inhibition in renal cell carcinoma
Author/Authors :
Pinto Marيn، نويسنده , , Alvaro and Redondo Sلnchez، نويسنده , , Andrés and Espinosa Arranz، نويسنده , , Enrique and Zamora Auٌَn، نويسنده , , Pilar and Castelo Fernلndez، نويسنده , , Beatriz and Gonzلlez Barَn، نويسنده , , Manuel، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2012
Pages :
6
From page :
356
To page :
361
Abstract :
Renal cell carcinoma therapy has changed in a very significant way in the last few years. Up to 5 new agents have been developed, improving the results previously achieved with cytokine therapy. Bevacizumab, sorafenib, sunitinib, temsirolimus, and everolimus are now part of the therapeutic arsenal for this illness. Particularly, this has been the first tumoral type in which inhibition of mammalian target of rapamycin (mTOR) has proved its efficacy in phase III trials, either as first-line therapy for poor prognosis patients (temsirolimus, CCI-779) or as second-line therapy after failure of tyrosine-kinase inhibitors (everolimus, RAD001). In this paper, we review the basis for mTOR inhibition in RCC, and discuss the results of the trials involving temsirolimus and everolimus for the treatment of this disease.
Keywords :
renal cell carcinoma , mTOR , Temsirolimus , Everolimus
Journal title :
Urologic Oncology
Serial Year :
2012
Journal title :
Urologic Oncology
Record number :
1890592
Link To Document :
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